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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417811생성일: 2026년 10월 25일

Thiodiglycol → 5-Hydroxy-3-thiapentyl N,N,N',N'-tetrakis(2-chloroethyl)phosphorodiamidate

https://huagongshe.com/reaction/417811

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참여 물질

역할이름HCID투입량
반응물ThiodiglycolHCID 5447—
반응물N,N,N',N'-Tetrakis(2-chloroethyl)phosphorodiamidic ChlorideHCID 428391—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-Hydroxy-3-thiapentyl N,N,N',N'-tetrakis(2-chloroethyl)phosphorodiamidateHCID 5916497042.6%

반응 조건

온도2.5 °C

반응 단계

N,N,N′,N′-Tetrakis(2-chloroethyl)phosphorodiamidoyl chloride, 636 mg (1.745 mmol), and bis(2-hydroxyethyl)sulfide, 1 mL (9.67 mmol), were dissolved in 8 mL anhydrous tetrahydrofuran and cooled to 0-5° C. in an ice-water bath. Potassium tert-butoxide, 1.8 mL of 1 M solution in tetrahydrofuran (1.8 mmol), was added over a 10 minute period, and the reaction mixture kept at 0-5° C. for another 30 minutes. The reaction mixture was allowed to warm to room temperature and stirred at room temperature for 18 hours. It was then diluted with ethyl acetate; and the ethyl acetate layer separated, washed with 1 M hydrochloric acid and brine, then dried over anhydrous magnesium sulfate, and the ethyl acetate removed under vacuum. The crude 5-hydroxy-3-thiapentyl N,N,N′,N′-tetrakis(2-chloroethyl)phosphorodiamidate was purified by column chromatography (silica gel, eluting with 25% ethyl acetate/hexane and 100% ethyl acetate), and obtained as a colorless oil, 335 mg (42.6% yield), identified by HPLC and 1H and 31P NMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093231B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-029e55fe4fae4964871431f209f3d083
출처 메모uspto-grants-2012_01